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PUBMED FOR HANDHELDS

Journal Abstract Search


307 related items for PubMed ID: 18363164

  • 1. Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxia.
    Adams SA, Steenblock KJ, Thibodeau SN, Lindor NM.
    J Neurogenet; 2008; 22(1):77-92. PubMed ID: 18363164
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  • 2. FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.
    Biancalana V, Toft M, Le Ber I, Tison F, Scherrer E, Thibodeau S, Mandel JL, Brice A, Farrer MJ, Dürr A.
    Arch Neurol; 2005 Jun; 62(6):962-6. PubMed ID: 15956167
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  • 4. Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
    Peters N, Kamm C, Asmus F, Holinski-Feder E, Kraft E, Dichgans M, Brüning R, Gasser T, Bötzel K.
    Mov Disord; 2006 Jan; 21(1):98-102. PubMed ID: 16124012
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  • 5. Fragile X premutation with atypical symptoms at onset.
    Cellini E, Forleo P, Ginestroni A, Nacmias B, Tedde A, Bagnoli S, Mascalchi M, Sorbi S, Piacentini S.
    Arch Neurol; 2006 Aug; 63(8):1135-8. PubMed ID: 16908740
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  • 6. Fragile X-associated tremor/ataxia syndrome (FXTAS).
    Hagerman PJ, Hagerman RJ.
    Ment Retard Dev Disabil Res Rev; 2004 Aug; 10(1):25-30. PubMed ID: 14994285
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  • 10. Parkinsonism, FXTAS, and FMR1 premutations.
    Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ.
    Mov Disord; 2005 Feb; 20(2):230-3. PubMed ID: 15390127
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  • 11. Fragile X-associated tremor/ataxia syndrome: intrafamilial variability and the size of the FMR1 premutation CGG repeat.
    Capelli LP, Gonçalves MR, Kok F, Leite CC, Nitrini R, Barbosa ER, Vianna-Morgante AM.
    Mov Disord; 2007 Apr 30; 22(6):866-70. PubMed ID: 17290448
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  • 20. FXTAS is rare among Portuguese patients with movement disorders: FMR1 premutations may be associated with a wider spectrum of phenotypes.
    Seixas AI, Vale J, Jorge P, Marques I, Santos R, Alonso I, Fortuna AM, Pinto-Basto J, Coutinho P, Margolis RL, Sequeiros J, Silveira I.
    Behav Brain Funct; 2011 Jun 03; 7():19. PubMed ID: 21639881
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